Genome scanning of the HXB/BXH sets of recombinant inbred strains of the rat for quantitative trait loci associated with conditioned taste aversion

被引:15
作者
Bielavská, E
Kren, V
Musilová, A
Zídek, V
Pravenec, M
机构
[1] Acad Sci Czech Republ, Inst Physiol, Prague 14220 4, Czech Republic
[2] Charles Univ Prague, Fac Med 1, Inst Biol & Med Genet, Prague, Czech Republic
关键词
QTL mapping; recombinant inbred strains; congenic strain; conditioned taste aversion; rat;
D O I
10.1023/A:1014407928865
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In the current study, we searched for quantitative trait loci (QTL) responsible for a conditioned taste aversion (CTA) measured as a decrease in the intake of a saccharin conditioned stimulus followed by an i.p. injection of 0.15 M LiCl (lithium chloride) (2 ml/100 g body weight). A genome scanning for QTL associated with CTA was performed in the HXB/BXH sets of recombinant inbred (RI) strains derived from the Brown Norway (BN-Lx) rat and the spontaneously hypertensive rat (SHR). The BN-Lx progenitor showed a significantly stronger CTA (8.3 +/- 2.8%) than the SHR progenitor (27.8 +/- 3.3%, p < .0001). The distribution of CTA values among RI strains was continuous, suggesting a polygenic mode of inheritance. Genome scanning of RI strains with more than 700 gene markers revealed a significant association of CTA with the D2Cebr1 l s4 marker on chromosome 2 (LRS = 22.7) and with the D4Cebrp149s8 marker on chromosome 4 (LRS = 23.4). The chromosome 2 putative QTL was confirmed by detecting a significant difference in CTA between the SHR progenitor (27.8 3.3%) and the SHR-2 (SHR.BN-D2Rat 171/D2Arb24) congenic strain (13.1 +/- 4.4%.p < .01) that are genetically identical except for a segment of chromosome 2 that was transferred onto the genetic background of the SHR from the BN strain.
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页码:51 / 56
页数:6
相关论文
共 30 条
[1]   Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats [J].
Aitman, TJ ;
Gotoda, T ;
Evans, AL ;
Imrie, H ;
Heath, KE ;
Trembling, PM ;
Truman, H ;
Wallace, CA ;
Rahman, A ;
Dore, C ;
Flint, J ;
Kren, V ;
Zidek, V ;
Kurtz, TW ;
Pravenec, M ;
Scott, J .
NATURE GENETICS, 1997, 16 (02) :197-201
[2]  
BAILEY DW, 1981, MOUSE BIOMEDICAL RES, V1, P223
[3]  
Bila V, 1996, FOLIA BIOL-PRAGUE, V42, P167
[4]  
Bores J, 1998, OXFORD PSYCHOL SERIE
[5]   Quantitative trait loci influencing cholesterol and phospholipid phenotypes map to chromosomes that contain genes regulating blood pressure in the spontaneously hypertensive rat [J].
Bottger, A ;
vanLith, HA ;
Kren, V ;
Krenova, D ;
Bila, V ;
Vorlicek, J ;
Zidek, V ;
Musilova, A ;
Zdobinska, M ;
Wang, JM ;
vanZutphen, BFM ;
Kurtz, TW ;
Pravenec, M .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (03) :856-862
[6]   An integrated genetic linkage map of the laboratory rat [J].
Brown D.M. ;
Matise T.C. ;
Koike G. ;
Simon J.S. ;
Winer E.S. ;
Zangen S. ;
McLaughlin M.G. ;
Shiozawa M. ;
Atkinson O.S. ;
Hudson Jr. J.R. ;
Chakravarti A. ;
Lander E.S. ;
Jacob H.J. .
Mammalian Genome, 1998, 9 (7) :521-530
[7]  
Buck KJ, 1997, J NEUROSCI, V17, P3946
[8]  
Bures J., 1988, Brain and behavior paradigms for research in neural mechanisms
[9]  
Doerge RW, 1996, GENETICS, V142, P285
[10]   CONTINUED DEVELOPMENT AND UNCONDITIONED STIMULUS CHARACTERIZATION OF SELECTIVELY BRED LINES OF TASTE-AVERSION PRONE AND RESISTANT RATS [J].
ELKINS, RL ;
WALTERS, PA ;
ORR, TE .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1992, 16 (05) :928-934